143 related articles for article (PubMed ID: 10762553)
21. Locus controlling LDL cholesterol response to dietary cholesterol is on baboon homologue of human chromosome 6.
Kammerer CM; Rainwater DL; Cox LA; Schneider JL; Mahaney MC; Rogers J; VandeBerg JL
Arterioscler Thromb Vasc Biol; 2002 Oct; 22(10):1720-5. PubMed ID: 12377755
[TBL] [Abstract][Full Text] [Related]
22. Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.
Fischer J; Faure A; Bouadjar B; Blanchet-Bardon C; Karaduman A; Thomas I; Emre S; Cure S; Ozgüc M; Weissenbach J; Prud'homme JF
Am J Hum Genet; 2000 Mar; 66(3):904-13. PubMed ID: 10712205
[TBL] [Abstract][Full Text] [Related]
23. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
Chen S; Ondo WG; Rao S; Li L; Chen Q; Wang Q
Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200
[TBL] [Abstract][Full Text] [Related]
24. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
Gelernter J; Bonvicini K; Page G; Woods SW; Goddard AW; Kruger S; Pauls DL; Goodson S
Am J Med Genet; 2001 Aug; 105(6):548-57. PubMed ID: 11496373
[TBL] [Abstract][Full Text] [Related]
25. Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease.
Gutiérrez-Cirlos C; Ordóñez-Sánchez ML; Tusié-Luna MT; Patterson BW; Schonfeld G; Aguilar-Salinas CA
Ann Hepatol; 2011; 10(2):155-64. PubMed ID: 21502677
[TBL] [Abstract][Full Text] [Related]
26. Comparison of genome screens for two independent cohorts provides replication of suggestive linkage of bone mineral density to 3p21 and 1p36.
Wilson SG; Reed PW; Bansal A; Chiano M; Lindersson M; Langdown M; Prince RL; Thompson D; Thompson E; Bailey M; Kleyn PW; Sambrook P; Shi MM; Spector TD
Am J Hum Genet; 2003 Jan; 72(1):144-55. PubMed ID: 12478480
[TBL] [Abstract][Full Text] [Related]
27. Identification of a new candidate locus for uric acid nephrolithiasis.
Ombra MN; Forabosco P; Casula S; Angius A; Maestrale G; Petretto E; Casu G; Colussi G; Usai E; Melis P; Pirastu M
Am J Hum Genet; 2001 May; 68(5):1119-29. PubMed ID: 11309680
[TBL] [Abstract][Full Text] [Related]
28. Linkage of Paget disease of bone to a novel region on human chromosome 18q23.
Good DA; Busfield F; Fletcher BH; Duffy DL; Kesting JB; Andersen J; Shaw JT
Am J Hum Genet; 2002 Feb; 70(2):517-25. PubMed ID: 11742440
[TBL] [Abstract][Full Text] [Related]
29. Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred.
Hunt SC; Hopkins PN; Bulka K; McDermott MT; Thorne TL; Wardell BB; Bowen BR; Ballinger DG; Skolnick MH; Samuels ME
Arterioscler Thromb Vasc Biol; 2000 Apr; 20(4):1089-93. PubMed ID: 10764678
[TBL] [Abstract][Full Text] [Related]
30. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study.
Coon H; Myers RH; Borecki IB; Arnett DK; Hunt SC; Province MA; Djousse L; Leppert MF
Arterioscler Thromb Vasc Biol; 2000 Oct; 20(10):2275-80. PubMed ID: 11031215
[TBL] [Abstract][Full Text] [Related]
31. A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: genetic and metabolic studies.
Srivastava N; Noto D; Averna M; Pulai J; Srivastava RA; Cole TG; Latour MA; Patterson BW; Schonfeld G
Metabolism; 1996 Oct; 45(10):1296-304. PubMed ID: 8843188
[TBL] [Abstract][Full Text] [Related]
32. Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method.
Camp NJ; Neuhausen SL; Tiobech J; Polloi A; Coon H; Myles-Worsley M
Am J Hum Genet; 2001 Dec; 69(6):1278-89. PubMed ID: 11668428
[TBL] [Abstract][Full Text] [Related]
33. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
Stöber G; Saar K; Rüschendorf F; Meyer J; Nürnberg G; Jatzke S; Franzek E; Reis A; Lesch KP; Wienker TF; Beckmann H
Am J Hum Genet; 2000 Nov; 67(5):1201-7. PubMed ID: 11001582
[TBL] [Abstract][Full Text] [Related]
34. Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
Hocking LJ; Herbert CA; Nicholls RK; Williams F; Bennett ST; Cundy T; Nicholson GC; Wuyts W; Van Hul W; Ralston SH
Am J Hum Genet; 2001 Nov; 69(5):1055-61. PubMed ID: 11555792
[TBL] [Abstract][Full Text] [Related]
35. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
36. The hypobetalipoproteinemias.
Schonfeld G
Annu Rev Nutr; 1995; 15():23-34. PubMed ID: 8527219
[TBL] [Abstract][Full Text] [Related]
37. Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.
Feather SA; Malcolm S; Woolf AS; Wright V; Blaydon D; Reid CJ; Flinter FA; Proesmans W; Devriendt K; Carter J; Warwicker P; Goodship TH; Goodship JA
Am J Hum Genet; 2000 Apr; 66(4):1420-5. PubMed ID: 10739767
[TBL] [Abstract][Full Text] [Related]
38. Molecular diagnosis of hypobetalipoproteinemia: an ENID review.
Tarugi P; Averna M; Di Leo E; Cefalù AB; Noto D; Magnolo L; Cattin L; Bertolini S; Calandra S
Atherosclerosis; 2007 Dec; 195(2):e19-27. PubMed ID: 17570373
[TBL] [Abstract][Full Text] [Related]
39. Family-based association analysis validates chromosome 3p21 as a putative nasopharyngeal carcinoma susceptibility locus.
Zeng Z; Zhou Y; Zhang W; Li X; Xiong W; Liu H; Fan S; Qian J; Wang L; Li Z; Shen S; Li G
Genet Med; 2006 Mar; 8(3):156-60. PubMed ID: 16540749
[TBL] [Abstract][Full Text] [Related]
40. Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote.
Hooper AJ; Robertson K; Champain D; Hua J; Song S; Parhofer KG; Barrett PHR; van Bockxmeer FM; Burnett JR
Clin Biochem; 2016 Jun; 49(9):720-722. PubMed ID: 26916057
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]